A. W. Behbehani

A familial progressive neurodegenerative disease with 2-oxoglutaric aciduria

Alfried Kohlsch�tter, A. W. Behbehani, U. Langenbeck et al. · European Journal of Pediatrics · 1982 · 61 citations

Neurodegenerative Diseases, Corticobasal Degeneration, Degenerative Disease +6

Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase

A. W. Behbehani, Hans H. Goebel, G. Osse et al. · European Journal of Pediatrics · 1984 · 38 citations

Mitochondrial Myopathy, Lactic Acidosis, Energy Metabolism +11

Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria

H. Böhles, Kurt Ullrich, W. Endres et al. · European Journal of Pediatrics · 1991 · 27 citations

Nutrition, Electrolyte Disorder, Possible Cause +7

Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of age

Ulrich Langenbeck, A. W. Behbehani, Angelika Mench-Hoinowski et al. · European Journal of Pediatrics · 1980 · 14 citations

Urology, Medicine, Pediatrics +5

Comparative column chromatographic estimations of phenylalanine in plasma, whole blood, native and paper‐dried capillary blood of healthy children and adults, and patients with hyperphenylalaninaemia

Kyra J. Becker, J. Harenz, N. Kalle et al. · Journal of Inherited Metabolic Disease · 1984 · 13 citations